Cytomegalovirus by Qualitative PCR, Saliva
Also known as: CMVPCR SAL
Use
This test detects the presence of cytomegalovirus (CMV) in saliva specimens using a qualitative PCR method. It does not quantify the viral load but is potentially useful for congenital screening of neonates to determine the presence of CMV-associated hearing loss. The test is suitable for clinical purposes as it is performed in a CLIA certified laboratory. However, it should be noted that the test is not cleared or approved by the FDA.
Special Instructions
The test requires saliva collected using the ORACollect OC-100 kit, which can be ordered online through ARUP eSupply or by contacting ARUP Client Services. Proper collection and transport are essential for accurate results.
Limitations
A negative result does not rule out the presence of PCR inhibitors in the patient specimen or the presence of nucleic acid at levels below the detection limit of the test. Additionally, as the test is not FDA approved, results should be interpreted with clinical correlation by well-trained personnel.
New York Approved
Methodology
PCR-based (qPCR)
Biomarkers
LOINC Codes
- 31208-2
- 83065-3
Result Turnaround Time
1-3 days
Related Documents
For more information, please review the documents below
Specimen
Saliva
Volume
Not provided
Minimum Volume
Not provided
Container
ORACollect OC-100 kit
Collection Instructions
Collect saliva using the ORACollect OC-100 kit. Transport in the same kit.
Storage Instructions
Store and transport the saliva specimen frozen.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 7 days |
| Frozen | 3 months |